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3(2H)-Pyridazinone

    • Product Name 3(2H)-Pyridazinone
    • Einecs 202-810-3
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    488509

    Iupac Name 3(2H)-Pyridazinone
    Molecular Formula C4H4N2O
    Molar Mass 96.09 g/mol
    Cas Number 480-94-4
    Appearance White to off-white solid
    Melting Point 138-141°C
    Boiling Point 360°C (estimated)
    Solubility In Water Slightly soluble
    Density 1.38 g/cm³ (estimated)
    Pubchem Cid 10244

    As an accredited 3(2H)-Pyridazinone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 100-gram amber glass bottle labeled “3(2H)-Pyridazinone”; features hazard symbols, chemical formula, and manufacturer details for laboratory use.
    Shipping 3(2H)-Pyridazinone is typically shipped in sealed, chemical-resistant containers to prevent moisture and contamination. Packaging complies with relevant hazardous material regulations. The containers are clearly labeled with appropriate hazard warnings. During transit, the chemical is handled according to safety guidelines to ensure stability and prevent spills or exposure.
    Storage 3(2H)-Pyridazinone should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from direct sunlight, heat sources, and incompatible substances such as strong oxidizers. It is important to avoid moisture and protect it from physical damage. Proper labeling and use of personal protective equipment when handling are recommended to ensure safety.
    Application of 3(2H)-Pyridazinone

    Applications of 3(2H)-Pyridazinone in Industrial Manufacturing

    3(2H)-Pyridazinone serves as a key intermediate for multiple specialized industries. Through controlled synthesis and targeted formulation, manufacturers leverage its molecular structure for high-value chemical processes and finished goods production. Below we detail major application segments where our plant-grade 3(2H)-Pyridazinone plays a critical role, aligned with sector-specific compliance and operational requirements.

    1. Pharmaceutical Intermediate Synthesis

    Major pharmaceutical manufacturers employ 3(2H)-Pyridazinone as a building block in API synthesis, especially for antihypertensive, anti-inflammatory, and psychotropic agents. The compound enters established production routes requiring stringent traceability and impurity control. Usually, it acts as a heterocyclic motif for late-stage functionalization under regulated GMP conditions, supporting the development of patented and generic molecules targeting CNS and cardiovascular indications.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU Guidelines for GMP (EudraLex Volume 4)
    • US FDA Current Good Manufacturing Practice (21 CFR Parts 210 and 211)
    • Chinese Pharmacopoeia (when used in China-market APIs)

    Typical usage ratio

    • Input load varies from 0.6 to 1.4 mol per mol of final API, based on route optimization and desired yield.

    Downstream process integration

    • Typically introduced in multi-step synthesis as a cyclization or acylation substrate, followed by purification and analysis in GMP suites.

    Final product types

    • Antihypertensive drug substances
    • Psychotropic active ingredients
    • Non-steroidal anti-inflammatory drug intermediates

    2. Crop Protection Chemicals Manufacturing

    Leading agrochemical producers incorporate 3(2H)-Pyridazinone into the development of selective herbicides and fungicides. The molecule’s pyridazinone backbone enhances biological activity and environmental stability. Global companies combine it via condensation and substitution steps, focusing on actives for resistant weed management and disease control. Strict absorption, residue, and environmental release tests shape formulation and registration processes.

    Industry compliance standards

    • FAO/WHO specifications for plant protection products
    • EU Regulation (EC) No 1107/2009 for pesticide approval
    • US EPA 40 CFR Part 180 – Tolerances for pesticide residues
    • OECD guidelines for chemical testing

    Typical usage ratio

    • Reactant/substrate ratio ranges from 0.8 to 1.2 equiv per active ingredient preparation, adjusted per biological performance screening results.

    Downstream process integration

    • Integrated in the core step of heterocyclic ring formation, further processed for granulation, encapsulation, or emulsion concentrates.

    Final product types

    • Pre-emergence and post-emergence herbicides
    • Systemic fungicidal formulations
    • Pesticide technical concentrates for export and domestic use

    3. Specialty Dyes and Pigments Synthesis

    Colorant and pigment manufacturers use 3(2H)-Pyridazinone as a core intermediate in synthesizing specialty dyes, benefiting from its electron-donating and chromophore-modifying features. It enters azine and hydrazone dye routes for applications in textile printing, plastics, and high-performance inks. Quality control checks target color fastness, purity, and absence of prohibited aromatic amines as demanded by international standards.

    Industry compliance standards

    • OEKO-TEX Standard 100 (textiles chemicals)
    • EN 71-3:2019 (toys, migration of certain elements)
    • REACH Regulation (EC) No 1907/2006 for chemical substances
    • ISO 9001:2015-certified pigment production quality systems

    Typical usage ratio

    • Colorant formulation range: 2–7% by mass of final dye or pigment, based on spectrophotometric profile requirements.

    Downstream process integration

    • Introduced during diazotization and coupling reactions, under strict temperature and pH control, then isolated by filtration or crystallization.

    Final product types

    • Disperse and vat dyes for textiles
    • Organic pigments for plastics and rubbers
    • Inkjet printer and specialty industrial inks

    4. Fine Chemical Building Blocks for Polymer Additives

    Producers specializing in polymer stabilizers and functional additives formulate 3(2H)-Pyridazinone for use in UV absorber and antioxidant blends. The chemical structure provides radical scavenging and light stabilization required in high-durability plastics, automotive coatings, and elastomers. Advanced QC quantifies migration, interaction byproducts, and shelf-life parameters following composite extrusion or molding processes.

    Industry compliance standards

    • EU Regulation (EC) No 10/2011 for food contact plastics
    • ISO 11357 (plastics—differential scanning calorimetry requirements)
    • ASTM D2565 for outdoor weathering simulation
    • RoHS Directive 2011/65/EU (restricted substances in electronics)

    Typical usage ratio

    • 0.1–0.5 phr (parts per hundred resin) in masterbatch concentrates, adjusted for target lifetime and expected UV exposure cycles.

    Downstream process integration

    • Blended in compounding or melt-extrusion, followed by let-down to application dose during downstream fabrication.

    Final product types

    • UV-stabilized polyethylene and polypropylene
    • Photostable polyurethane coatings
    • Elastomer-based cable sheaths and automotive trim parts
    Free Quote

    Competitive 3(2H)-Pyridazinone prices that fit your budget—flexible terms and customized quotes for every order.

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